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Visual Stimulus-Based Cognitive-Motor Agility Exercise in Older Adults

18 juli 2026 bijgewerkt door: Gulsah Sahin, Çanakkale Onsekiz Mart University

Effects of Visual Stimulus-Based Cognitive-Motor Agility Exercise on Cognitive, Psychomotor, and Functional Performance in Older Adults: A Randomized Controlled Trial

This randomized controlled trial examined the effects of adding a brief visual stimulus-based cognitive-motor agility exercise component to a multicomponent exercise program in community-dwelling older adults. Participants were randomized to either an experimental group or an active control group. Both groups participated in supervised multicomponent exercise sessions twice weekly for 8 weeks. Each session lasted 45 minutes. During the final 10 minutes of each session, the experimental group performed the visual stimulus-based cognitive-motor agility exercises, whereas the active control group performed time-matched low-intensity activities. The primary outcome was global cognitive performance assessed using the Montreal Cognitive Assessment. Secondary outcomes included hand and foot visual-motor response time, visual working memory, and functional performance.

Studie Overzicht

Gedetailleerde beschrijving

This study was designed as an 8-week, parallel-group randomized controlled exercise intervention in community-dwelling older adults. The study aimed to determine whether adding a brief Light Trainer-assisted visual stimulus-based cognitive-motor agility exercise component to a multicomponent exercise program would provide additional benefits for cognitive, psychomotor, and functional performance.

After completion of baseline assessments, eligible participants were randomized to either an experimental group or an active control group. Both groups participated in supervised exercise sessions twice weekly for 8 weeks, for a total of 16 sessions. Each session lasted 45 minutes. The first 35 minutes of each session consisted of the same multicomponent exercise program in both groups. This program included light-paced walking, mobility exercises, multidirectional stepping, balance tasks, agility exercise, coordination exercises, low-resistance strengthening exercises, and functional movement combinations.

During the final 10 minutes of each session, participants in the experimental group completed visual stimulus-based cognitive-motor agility exercises using the Light Trainer system. These tasks required participants to perceive randomized visual stimuli, select an appropriate motor response, and respond as quickly and accurately as possible using hand or foot movements. The Light Trainer component included 13 repetitions of 30-second task intervals separated by 15-second rest periods. Task difficulty progressed across the 8-week intervention by increasing the number of modules from two to six and by increasing task complexity, stimulus randomness, movement direction changes, response speed requirements, and cognitive-motor demands.

Participants in the active control group completed the same 35-minute multicomponent exercise program followed by a time-matched 10-minute low-intensity activity period. These activities included supervised stretching, mobility, agility, balance, or recovery exercises and did not include visual stimulus-based response tasks, rapid decision-making, reactive agility tasks, or Light Trainer-assisted exercises.

Assessments were performed at baseline and after the 8-week intervention period. The primary outcome was global cognitive performance assessed using the Montreal Cognitive Assessment. Secondary outcomes included hand and foot visual-motor response time, visual working memory performance time and accuracy, Ten-Step Test, 30-second Chair Stand Test, 30-second Arm Curl Test, and 8-Foot Up-and-Go Test. The study was conducted in community-dwelling older adults aged 60 years or older who were able to ambulate independently and follow basic exercise and testing instructions.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

41

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Çanakkale, Turkije (Türkiye), 17100
        • Çanakkale Onsekiz Mart University

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion Criteria:

  • Community-dwelling older adults aged 60 years or older
  • Able to ambulate independently
  • Able to understand and follow basic exercise and testing instructions
  • Montreal Cognitive Assessment score of 23 or higher
  • No health condition that would limit safe participation in exercise
  • Able to participate regularly in the 8-week exercise program

Exclusion Criteria:

  • Serious cardiovascular, neurological, orthopedic, or vestibular disease that could prevent safe participation in exercise
  • Recent surgery
  • Uncontrolled hypertension
  • Severe visual or hearing problems
  • Montreal Cognitive Assessment score below 23
  • Use of medications known to substantially affect cognitive, psychomotor, balance, or motor performance
  • Very low physical function preventing safe participation in the exercise program

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ander
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Visual stimuli Cognitive-Motor Agility Exercise
Participants in this arm completed supervised exercise sessions twice weekly for 8 weeks. Each 45-minute session included the same 35-minute multicomponent exercise program performed by both groups, followed by 10 minutes of Light Trainer-assisted visual stimulus-based cognitive-motor agility exercise. The Light Trainer component included reactive visual-motor tasks requiring participants to respond to randomized visual stimuli using hand and foot movements.
Participants completed a supervised 35-minute multicomponent exercise program twice weekly for 8 weeks. The program included light-paced walking, mobility exercises, multidirectional stepping, balance tasks, coordination exercises, low-resistance strengthening exercises, and functional movement combinations. This component was performed by both the experimental and active control groups.
The experimental group completed a 10-minute Light Trainer-assisted visual stimulus-based cognitive-motor agility exercise component during the final part of each supervised session. Tasks required participants to perceive randomized visual stimuli, select an appropriate motor response, and respond as quickly and accurately as possible using hand or foot movements. Each session included 13 repetitions of 30-second task intervals separated by 15-second rest periods. Task difficulty progressed across 8 weeks by increasing the number of modules from two to six and increasing task complexity.
Actieve vergelijker: Active Control: Multicomponent Exercise With Low-Intensity Activities
Participants in this arm completed supervised exercise sessions twice weekly for 8 weeks. Each 45-minute session included the same 35-minute multicomponent exercise program performed by the experimental group, followed by 10 minutes of time-matched low-intensity activities. These activities included supervised stretching, mobility, balance, or recovery exercises and did not include visual stimulus-based response tasks, rapid decision-making, reactive agility tasks, or Light Trainer-assisted exercises.
Participants completed a supervised 35-minute multicomponent exercise program twice weekly for 8 weeks. The program included light-paced walking, mobility exercises, multidirectional stepping, balance tasks, coordination exercises, low-resistance strengthening exercises, and functional movement combinations. This component was performed by both the experimental and active control groups.
The active control group completed a 10-minute time-matched low-intensity activity period during the final part of each supervised session. These activities included stretching, mobility, balance, or recovery exercises and did not include visual stimulus-based response tasks, rapid decision-making, reactive agility tasks, or Light Trainer-assisted exercises.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Montreal Cognitive Assessment Score
Tijdsspanne: Baseline and 8 weeks
The Montreal Cognitive Assessment was used to assess global cognitive function. Scores range from 0 to 30, with higher scores indicating better cognitive performance. Change from baseline to 8 weeks was evaluated. The Montreal Cognitive Assessment was used to assess global cognitive function. Scores range from 0 to 30, with higher scores indicating better cognitive performance. Change from baseline to 8 weeks was evaluated.
Baseline and 8 weeks

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in Ten-Step Test Time
Tijdsspanne: Baseline and after 8 weeks
Lower-extremity rapid stepping and agility performance were assessed using the Ten-Step Test. Participants completed 10 alternating stepping movements on a 10-cm step block as quickly as possible. Test duration was recorded in seconds. Shorter time indicates better performance.
Baseline and after 8 weeks
Change in Hand Visual-Motor Response Time
Tijdsspanne: Baseline and 8 weeks
Hand visual-motor response performance was assessed using the Light Trainer system. Participants responded to randomized visual stimuli by touching illuminated modules with either hand during a 30-second task. Fastest and mean response times were recorded in seconds. Shorter response times indicate better performance.
Baseline and 8 weeks
Change in Foot Visual-Motor Response Time
Tijdsspanne: Baseline and 8 weeks
Foot visual-motor response performance was assessed using the Light Trainer system. Participants responded to randomized visual stimuli by stepping on illuminated modules with either foot during a 30-second task. Fastest and mean response times were recorded in seconds. Shorter response times indicate better performance.
Baseline and 8 weeks
Change in Visual Working Memory Performance Time
Tijdsspanne: Baseline and 8 weeks
Visual working memory response time was assessed using the memory mode of the Light Trainer system. Participants memorized the color and position of illuminated modules and then identified the module corresponding to a target color. Fastest times were recorded in seconds, with shorter values indicating better visual working memory performance. Change from baseline to 8 weeks was evaluated.
Baseline and 8 weeks
Change in Visual Working Memory Accuracy
Tijdsspanne: Baseline and 8 weeks
Visual working memory accuracy was assessed using the memory mode of the Light Trainer system. Participants memorized the color and position of illuminated modules and then identified the module corresponding to a target color. Accuracy was expressed as the device-recorded percentage of correct responses across all trials and ranged from 0% to 100%, with higher values indicating better visual working memory performance. Change from baseline to 8 weeks was evaluated.
Baseline and 8 weeks
Change in 30-Second Chair Stand Test Performance
Tijdsspanne: Baseline and 8 weeks
Lower-body functional strength was assessed using the 30-second Chair Stand Test. Participants were instructed to stand up fully and sit down as many times as possible within 30 seconds. The total number of correctly completed repetitions was recorded. Higher repetition count indicates better performance.
Baseline and 8 weeks
Change in 30-Second Arm Curl Test Performance
Tijdsspanne: Baseline and 8 weeks
Upper-body functional strength was assessed using the 30-second Arm Curl Test. Participants performed as many controlled elbow flexion-extension repetitions as possible within 30 seconds while seated. The test was performed separately for the right and left arms. Higher repetition count indicates better performance.
Baseline and 8 weeks
Change in 8-Foot Up-and-Go Test Time
Tijdsspanne: Baseline and 8 weeks
Functional mobility, agility, and dynamic balance were assessed using the 8-Foot Up-and-Go Test. Participants rose from a chair, walked around a marker placed 2.44 meters away, returned to the chair, and sat down again. Test duration was recorded in seconds. Shorter time indicates better performance.
Baseline and 8 weeks

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 april 2026

Primaire voltooiing (Werkelijk)

8 juni 2026

Studie voltooiing (Werkelijk)

8 juni 2026

Studieregistratiedata

Eerst ingediend

15 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

15 juli 2026

Eerst geplaatst (Werkelijk)

20 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

21 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

18 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • 2026-YONP-0051

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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